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Tremorine-oxotremorine-induced tremor, hypothermia and analgesia, and physostigmine toxicity, in mice after pretreatment with β-adrenoceptor antagonists
14
Citations
26
References
1976
Year
Tremorine-oxotremorine-induced TremorPharmacotherapyExperimental PharmacologyMolecular PharmacologyMedicinal ChemistryAnesthetic PharmacologyBehavioral PharmacologyWhereas PronethalolNeuropharmacologyPharmacological AgentAnesthesiologyPharmacologyAnti-tremor ActivityPhysiologyCentral Anticholinergic ActivityPhysostigmine ToxicityAnesthesiaMedicineβ-Adrenoceptor AntagonistsDrug DiscoveryAlpha-adrenergic Pharmacology
Abstract The β-adrenoceptor blockers propranolol, PhQA33 and LB-46 exhibited appreciable activity against tremorine-(TMN) and oxotremorine-(OTMN) induced tremor, whereas pronethalol, (+)-H56/28, (–)-H56/28, KÖ-592 and l(+)-INPEA possessed weak action. The two β-blockers, namely d,l(±)-INPEA and d(–)-INPEA acted as weak tremorgens. None of the above compounds suppressed the induced peripheral cholinergic phenomena; or possessed any central anticholinergic activity, as they were unable to afford protection against physostigmine-induced death. Propranolol, PhQA33 and LB-46 antagonized TMN-induced hypothermia and analgesia, but were inactive against OTMN-induced changes. A correlation of the β-blocking and anti-tremor activity of these agents is unlikely.
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